MAUDE Adverse Event Report: C.R. BARD, INC. (BASD) -3006260740 POWERPICC SHERLOCK 3CG BARD MYPICC KIT (5F) (DUAL-LUMEN) (TPS); CATHETER,INTRAVASCULAR,THERAPEUTIC,LONG-TERM GREATER THAN 30 DAYS

Model Number	N/A
Health Effect - Clinical Code	No Consequences Or Impact To Patient (2199)
Date of Event	01/09/2021
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
The device has not been returned to the manufacturer for evaluation.A lot history review (lhr) of 20ebe395 showed no other similar product complaint(s) from this lot number.
Event or Problem Description
It was reported "when picc was being inserted, the wire was not going smoothly.Rn was inserting, pulling back, re-inserting due to resistance.Finally pulled entire picc out and noticed that approx 1 inch of wire was missing.Patient received multiple x-rays and ct scans to locate wire.As of (b)(6), no wire was located in patient.Rn had thrown away the picc / wire once it was removed from patient.".

• Brand Name: POWERPICC SHERLOCK 3CG BARD MYPICC KIT (5F) (DUAL-LUMEN) (TPS)
• Common Device Name: CATHETER,INTRAVASCULAR,THERAPEUTIC,LONG-TERM GREATER THAN 30 DAYS
• Manufacturer (Section D): C.R. BARD, INC. (BASD) -3006260740; 605 north 5600 west; salt lake city 84116
• MDR Report Key: 11282604
• Report Number: 3006260740-2021-00231
• Device Sequence Number: 19066089
• Product Code: LJS
• UDI-Device Identifier: 00801741042973
• UDI-Public: (01)00801741042973
• Combination Product (Y/N): N
• Initial Reporter State: NJ
• Initial Reporter Country: US
• PMA/510(K) Number: K091324
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2021
• Reporter Type: Manufacturer
• Report Source: company representative,other
• Initial Reporter Occupation: Other Health Care Professional
• Type of Report: Initial
• Report Date (Section B): 01/14/2021

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Operator of Device: Health Professional
• Device Model Number: N/A
• Device Catalogue Number: CK000171
• Device Lot Number: 20EBE395
• Was Device Available for Evaluation?: No
• Type of Report(Section G): Initial
• Initial Date Received by Manufacturer: 01/11/2021
• Initial Report FDA Received Date: 02/04/2021
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1
• Outcome Attributed to Adverse Event: Other